This holiday season, give Jack hope for a brighter future.
Gifts made to Cure JM Foundation in honor of Jack will be matched by the Leetz Family Match.
In June, Jack was diagnosed with Juvenile Myositis, and his young life was turned upside down. This disease changes everything. The child faces a body fighting itself. Juvenile Myositis can attack any system of the body.
There are currently no FDA-approved treatments. There is no cure...yet. But we can change that.
Like most rare diseases, JM research funding comes almost entirely from grassroots efforts like these fundraising pages.
Why does your gift of hope matter?
All gifts go straight to Cure JM Foundation and will support crucial work, including:
· Making JM research at 24 major institutions around the world possible
· Funding drug discovery and development research, so children will have more and better treatments
· Investing in research to understand the genes that contribute to JM
· Finding and supporting the “best and the brightest” of the next generation of doctors and researchers that will support and treat our children
We are forever grateful to you and your support. It means so much to us.
Whatever level of support you can consider, please know that we will put it to work at the earliest possible moment to find better treatments.
We always say, “A Cure Can’t Wait.”
Neither can kids like Jack.
We’re so grateful to you. Thank you for giving the gift of hope this holiday season.